首页> 美国卫生研究院文献>Journal of Interferon Cytokine Research >Identification of 2′-5′-Oligoadenylate Synthetase-Like Gene in Goose: Gene Structure Expression Patterns and Antiviral Activity Against Newcastle Disease Virus
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Identification of 2′-5′-Oligoadenylate Synthetase-Like Gene in Goose: Gene Structure Expression Patterns and Antiviral Activity Against Newcastle Disease Virus

机译:鹅中2-5-寡腺苷酸合成酶样基因的鉴定:基因结构表达模式和对新城疫病毒的抗病毒活性

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摘要

2′-5′-oligoadenylate synthetase-like (OASL) is a kind of antiviral protein induced by interferons (IFNs), which plays an important role in the IFNs-mediated antiviral signaling pathway. In this study, we cloned and identified OASL in the Chinese goose for the first time. Goose 2′-5′-oligoadenylate synthetase-like (goOASL), including an ORF of 1527bp, encoding a protein of 508 amino acids. GoOASL protein contains 3 conserved motifs: nucleotidyltransferase (NTase) domain, 2′-5′-oligoadenylate synthetase (OAS) domain, and 2 ubiquitin-like (UBL) repeats. The tissue distribution profile of goOASL in 2-week-old gosling and adult goose were identified by Real-Time quantitative PCR, which revealed that the highest level of goOASL mRNA transcription was detected in the blood of adult goose and gosling. The mRNA transcription level of goOASL was upregulated in all tested tissues of duck Tembusu virus (DTMUV)-infected 3-day-old goslings, compared with control groups. Furthermore, using the stimulus Poly(I: C), ODN2006, R848, and lipopolysaccharide (LPS) as well as the viral pathogens DTMUV, H9N2 avian influenza virus (AIV), and gosling plague virus (GPV) to treat goose peripheral blood mononuclear cells (PBMCs) for 6 h, goOASL transcripts level was significantly upregulated in all treated groups. To further investigate the antiviral activity of goOASL, pcDNA3.1(+)-goOASL-His plasmid was constructed, and goOASL was expressed by the goose embryo fibroblast cells (GEFs) transfected with pcDNA3.1(+)-goOASL-His. Our research data suggested that Newcastle disease virus (NDV) replication (viral copies and viral titer) in GEFs was significantly reduced by the overexpression of goOASL protein. These data were meaningful for the antiviral immunity research of goose and shed light on the future prevention of NDV in fowl.
机译:2′-5′-寡腺苷酸合成酶样(OASL)是一种由干扰素(IFN)诱导的抗病毒蛋白,在IFNs介导的抗病毒信号通路中起着重要的作用。在这项研究中,我们首次在中国鹅中克隆并鉴定了OASL。鹅2'-5'-寡腺苷酸合成酶样(goOASL),包含1527bp的ORF,编码508个氨基酸的蛋白质。 GoOASL蛋白包含3个保守的基序:核苷酸转移酶(NTase)域,2'-5'-寡腺苷酸合成酶(OAS)域和2个泛素样(UBL)重复序列。通过实时定量PCR鉴定了2周龄小鹅和成年鹅中goOASL的组织分布图,这表明成年鹅和小鹅的血液中goOASL mRNA转录水平最高。与对照组相比,在感染了3天大的雏鸭鹅的Tembusu病毒(DTMUV)感染的所有测试组织中,goOASL的mRNA转录水平均上调。此外,使用刺激性Poly(I:C),ODN2006,R848和脂多糖(LPS)以及病毒病原体DTMUV,H9N2禽流感病毒(AIV)和小鹅瘟病毒(GPV)来治疗鹅外周血单个核在所有处理组中,细胞(PBMC)持续6 h,goOASL转录水平均显着上调。为了进一步研究goOASL的抗病毒活性,构建了pcDNA3.1(+)-goOASL-His质粒,并通过转染pcDNA3.1(+)-goOASL-His的鹅胚成纤维细胞(GEF)表达goOASL。我们的研究数据表明,goOASL蛋白的过表达显着降低了GEF中的新城疫病毒(NDV)复制(病毒拷贝和病毒滴度)。这些数据对于鹅的抗病毒免疫研究具有重要意义,并为未来家禽NDV的预防提供了参考。

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